Variant report

Variant	nsv432652
Chromosome Location	chr4:152791533-152818018
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:203)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:152808277-152809195	GM12878	blood:	n/a	n/a
2	ATF2	chr4:152809281-152810219	GM12878	blood:	n/a	n/a
3	ATF2	chr4:152809343-152810130	GM12878	blood:	n/a	n/a
4	ATF2	chr4:152803022-152804149	GM12878	blood:	n/a	n/a
5	ATF2	chr4:152808205-152809175	GM12878	blood:	n/a	n/a
6	ATF2	chr4:152803112-152804069	GM12878	blood:	n/a	n/a
7	BATF	chr4:152808574-152808994	GM12878	blood:	n/a	n/a
8	BATF	chr4:152808319-152808968	GM12878	blood:	n/a	n/a
9	BATF	chr4:152803669-152804037	GM12878	blood:	n/a	chr4:152803880-152803890
10	BATF	chr4:152803353-152804151	GM12878	blood:	n/a	chr4:152803510-152803523 chr4:152803880-152803890
11	BATF	chr4:152809440-152809995	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:152808382-152808996	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:152795348-152795763	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr4:152809611-152810010	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:152803271-152803628	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:152795463-152795749	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr4:152803677-152804055	GM12878	blood:	n/a	chr4:152803878-152803887
18	BCL11A	chr4:152808349-152808937	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:152809516-152810105	GM12878	blood:	n/a	n/a
20	BCL3	chr4:152809392-152810015	GM12878	blood:	n/a	n/a
21	BCLAF1	chr4:152809441-152810002	GM12878	blood:	n/a	n/a
22	BCLAF1	chr4:152803493-152804073	GM12878	blood:	n/a	chr4:152803878-152803887
23	BCLAF1	chr4:152808362-152809124	GM12878	blood:	n/a	n/a
24	BCLAF1	chr4:152808369-152808991	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:152808376-152809146	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:152803276-152804021	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:152806046-152806143	K562	blood:	n/a	chr4:152806107-152806120 chr4:152806109-152806118 chr4:152806109-152806118 chr4:152806108-152806117
28	BHLHE40	chr4:152809448-152810269	GM12878	blood:	n/a	n/a
29	CEBPB	chr4:152809313-152810190	GM12878	blood:	n/a	n/a
30	CHD1	chr4:152803862-152804116	GM12878	blood:	n/a	n/a
31	CHD2	chr4:152803533-152804150	GM12878	blood:	n/a	n/a
32	CHD2	chr4:152808440-152809021	GM12878	blood:	n/a	n/a
33	CHD2	chr4:152809457-152810107	GM12878	blood:	n/a	n/a
34	CHD2	chr4:152795494-152795803	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr4:152809880-152810030	GM12871	blood:	n/a	n/a
36	CTCF	chr4:152815213-152815276	Medullo	brain:	n/a	n/a
37	CTCF	chr4:152809820-152809970	GM12864	blood:	n/a	n/a
38	CTCF	chr4:152809840-152809990	GM12872	blood:	n/a	n/a
39	CTCF	chr4:152809720-152809870	GM12865	blood:	n/a	n/a
40	CTCF	chr4:152809820-152809970	GM12873	blood:	n/a	n/a
41	CTCF	chr4:152809660-152809810	GM12872	blood:	n/a	n/a
42	CTCF	chr4:152809712-152809940	GM12878	blood:	n/a	n/a
43	CTCF	chr4:152809800-152809950	GM12865	blood:	n/a	n/a
44	CTCF	chr4:152808720-152808870	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr4:152815899-152815956	GM20000	blood:	n/a	n/a
46	CTCF	chr4:152812500-152812650	GM12873	blood:	n/a	n/a
47	CTCF	chr4:152809740-152809890	GM12878	blood:	n/a	n/a
48	CTCF	chr4:152804016-152804059	GM12891	blood:	n/a	n/a
49	CTCF	chr4:152809560-152809710	GM12872	blood:	n/a	n/a
50	CTCF	chr4:152809800-152809950	GM12875	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:152801238-152801288	HCM	heart:	n/a
2	chr4:152801238-152801288	HRE	kidney:	n/a
3	chr4:152801238-152801288	RPTEC	kidney:	n/a
4	chr4:152801238-152801288	MCF-7	breast:	n/a
5	chr4:152808142-152808192	HL-60	blood:	n/a
6	chr4:152801238-152801288	HEK293	kidney:	embryo
7	chr4:152808142-152808192	BJ	skin:	n/a
8	chr4:152801238-152801288	Hela-S3	cervix:	n/a
9	chr4:152808142-152808192	NH-A	brain:	n/a
10	chr4:152808142-152808192	LNCaP	prostate:	n/a
11	chr4:152808142-152808192	CMK	blood:	n/a
12	chr4:152801238-152801288	HIPEpiC	eye:	n/a
13	chr4:152808142-152808192	GM06990	blood:	n/a
14	chr4:152808142-152808192	Hela-S3	cervix:	n/a
15	chr4:152801238-152801288	BE2_C	brain:	n/a
16	chr4:152801238-152801288	AG04449	skin:	fetal
17	chr4:152808142-152808192	Caco-2	colon:	n/a
18	chr4:152808142-152808192	BE2_C	brain:	n/a
19	chr4:152801238-152801288	AoSMC	blood vessel:	n/a
20	chr4:152801238-152801288	SK-N-SH_RA	brain:	n/a
21	chr4:152801238-152801288	NT2-D1	testis:	n/a
22	chr4:152808142-152808192	SK-N-MC	brain:	n/a
23	chr4:152801238-152801288	AG09319	gingival:	n/a
24	chr4:152808142-152808192	HRCEpiC	kidney:	n/a
25	chr4:152801238-152801288	AG04450	lung:	fetal
26	chr4:152808142-152808192	SAEC	small airway:	n/a
27	chr4:152808142-152808192	ProgFib	skin:	n/a
28	chr4:152808142-152808192	NB4	blood:	n/a
29	chr4:152801238-152801288	Jurkat	blood:	n/a
30	chr4:152808142-152808192	HCT-116	colon:	n/a
31	chr4:152801238-152801288	NHDF-neo	bronchial:	n/a
32	chr4:152801238-152801288	NHBE	bronchial:	n/a
33	chr4:152808142-152808192	SKMC	muscle:	n/a
34	chr4:152808142-152808192	HepG2	liver:	n/a
35	chr4:152801238-152801288	GM12892	blood:	n/a
36	chr4:152808142-152808192	NHDF-neo	bronchial:	n/a
37	chr4:152808142-152808192	AG09309	skin:	n/a
38	chr4:152808142-152808192	AoSMC	blood vessel:	n/a
39	chr4:152801238-152801288	PFSK-1	brain:	n/a
40	chr4:152801238-152801288	Hepatocyte	liver:	n/a
41	chr4:152801238-152801288	SK-N-MC	brain:	n/a
42	chr4:152801238-152801288	ovcar-3	ovarian:	n/a
43	chr4:152808142-152808192	SK-N-SH_RA	brain:	n/a
44	chr4:152808142-152808192	Hepatocyte	liver:	n/a
45	chr4:152808142-152808192	AG09319	gingival:	n/a
46	chr4:152808142-152808192	HEK293	kidney:	embryo
47	chr4:152808142-152808192	MCF10A-Er-Src	breast:	n/a
48	chr4:152808142-152808192	A549	lung:	n/a
49	chr4:152801238-152801288	SKMC	muscle:	n/a
50	chr4:152801238-152801288	HNPCEpiC	eye:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:152803737..152805745-chr4:152816897..152818541,2	MCF-7	breast:
2	chr4:152805506..152807725-chr4:152813069..152815634,2	K562	blood:
3	chr4:152791629..152793817-chr4:152795687..152797994,2	K562	blood:
4	chr4:152804097..152806378-chr4:152817285..152819187,2	K562	blood:
5	chr4:152804253..152807006-chr4:152811957..152814569,2	K562	blood:
6	chr4:152803724..152805338-chr4:152808624..152810923,2	K562	blood:
7	chr4:152791629..152793817-chr4:152795687..152797994,2	K562	blood:
8	chr4:152803724..152805338-chr4:152808624..152810923,2	K562	blood:
9	chr4:152804097..152806378-chr4:152817285..152819187,2	K562	blood:
10	chr4:152805506..152807725-chr4:152813069..152815634,2	K562	blood:
11	chr4:152803737..152805745-chr4:152816897..152818541,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PET112-1	chr4:152809643-152809730	XLOC_004123
2	lnc-FAM160A1-10	chr4:152810553-152811090	l_2755_chr4:152807157-152811090_testes
3	lnc-FAM160A1-10	chr4:152808057-152810405	l_2755_chr4:152807157-152811090_testes
4	lnc-PET112-1	chr4:152812319-152812415	XLOC_004123
5	lnc-FAM160A1-10	chr4:152807158-152808055	l_2755_chr4:152807157-152811090_testes
6	lnc-PET112-2	chr4:152812382-152812481	NONHSAT098772
7	lnc-PET112-1	chr4:152808695-152808915	XLOC_004123
8	lnc-PET112-2	chr4:152812455-152812481	XLOC_004124

No data

Variant related genes	Relation type
ENSG00000249708	TF binding region
ENSG00000249708	CpG island
ENSG00000249708	chromatin interactions
ZFYVE26	miRNA target sites

Extended variants
information (count: 1099 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17028001	chr4:152791533-152791534	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75001435	chr4:152791589-152791590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs17028004	chr4:152791654-152791655	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs552684550	chr4:152791670-152791671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571105015	chr4:152791687-152791688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375008719	chr4:152791746-152791747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550356914	chr4:152791765-152791766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs3885815	chr4:152791766-152791767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs77014847	chr4:152791783-152791784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187206110	chr4:152791792-152791793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566440772	chr4:152791798-152791799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150047482	chr4:152791815-152791816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545699087	chr4:152791818-152791819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6815081	chr4:152791830-152791831	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs146632420	chr4:152791839-152791840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544002511	chr4:152791873-152791874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs41400546	chr4:152791913-152791914	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs574663172	chr4:152791944-152791945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs41434145	chr4:152791979-152791980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs79903033	chr4:152791988-152791989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527684185	chr4:152792005-152792006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72732126	chr4:152792006-152792007	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs79183593	chr4:152792031-152792032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531792917	chr4:152792075-152792076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75228154	chr4:152792083-152792084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550626759	chr4:152792085-152792086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568622866	chr4:152792124-152792125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529587979	chr4:152792188-152792189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548065210	chr4:152792245-152792246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34413715	chr4:152792254-152792255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141461046	chr4:152792304-152792305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552052405	chr4:152792313-152792314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562824799	chr4:152792324-152792325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533550540	chr4:152792335-152792336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558081119	chr4:152792379-152792380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570231191	chr4:152792407-152792408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537515457	chr4:152792424-152792425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs116106942	chr4:152792426-152792427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386680776	chr4:152792438-152792439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369850217	chr4:152792462-152792463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530253557	chr4:152792484-152792485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535431043	chr4:152792493-152792494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554026960	chr4:152792495-152792496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145216172	chr4:152792530-152792531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13145151	chr4:152792546-152792547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs560670143	chr4:152792559-152792560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189715309	chr4:152792606-152792607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564446771	chr4:152792607-152792608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73862594	chr4:152792684-152792685	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs72732128	chr4:152792686-152792687	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:74)

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
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	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
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17588203	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152781200-152794800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:152789000-152796200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:152789400-152793800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:152791400-152800200	Weak transcription	Fetal Brain Male	brain
5	chr4:152793800-152794000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:152793800-152794000	Enhancers	Thymus	Thymus
7	chr4:152794000-152794400	Weak transcription	Aorta	Aorta
8	chr4:152794000-152795000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:152794600-152796800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:152794800-152795600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr4:152794800-152796400	Enhancers	H9 Cell Line	embryonic stem cell
12	chr4:152794800-152796400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr4:152794800-152796600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr4:152794800-152796600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:152794800-152796600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr4:152794800-152797400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr4:152795000-152796600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr4:152795000-152796600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr4:152795000-152798000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:152795400-152796400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr4:152795600-152796000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:152795600-152796000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr4:152795600-152796000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr4:152795800-152796400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:152795800-152798000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:152796000-152796600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:152796000-152799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:152796000-152801000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr4:152796200-152796600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr4:152796200-152796800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:152796400-152799600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr4:152796400-152800200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:152796400-152808200	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr4:152796600-152799600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr4:152796600-152800400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr4:152796600-152800600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr4:152796600-152806800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr4:152796600-152807200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr4:152796800-152797000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:152796800-152800200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr4:152797000-152798000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:152797400-152800200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr4:152798000-152800000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:152798000-152801600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:152799200-152799800	Enhancers	Brain Germinal Matrix	brain
46	chr4:152799600-152801600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr4:152799600-152802200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr4:152799800-152800800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:152799800-152801000	Weak transcription	Brain Germinal Matrix	brain
50	chr4:152799800-152803000	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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